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Volumn 17, Issue 6, 2012, Pages 6832-6839

Strong inhibition of Celastrol towards UDP-glucuronosyl transferase (UGT) 1A6 and 2B7 indicating potential risk of UGT-based herb-drug interaction

Author keywords

Celastrol; Herb drug interaction; UDP glucuronosyltransferase (UGT)

Indexed keywords

4-METHYLUMBELLIFERONE; DRUG DERIVATIVE; ENZYME INHIBITOR; GLUCURONOSYLTRANSFERASE; HYMECROMONE; TRIPTERINE; TRITERPENE; UDP GLUCURONOSYLTRANSFERASE, UGT1A6; UDP-GLUCURONOSYLTRANSFERASE, UGT1A6; UGT2B7 PROTEIN, HUMAN;

EID: 84862980316     PISSN: None     EISSN: 14203049     Source Type: Journal    
DOI: 10.3390/molecules17066840     Document Type: Article
Times cited : (35)

References (26)
  • 1
    • 19544390715 scopus 로고    scopus 로고
    • Herbal medications commonly used in the practice of rheumatology: Mechanisms of action, efficacy, and side effects
    • DOI 10.1016/j.semarthrit.2005.01.011, PII S0049017205000120
    • Setty, A. R.; Sigal, L. H. Herbal medications commonly used in the practice of rheumatology: Mechanisms of action, efficacy, and side effects. Semin. Arthritis Rheum. 2005, 34, 773-784. (Pubitemid 40732452)
    • (2005) Seminars in Arthritis and Rheumatism , vol.34 , Issue.6 , pp. 773-784
    • Setty, A.R.1    Sigal, L.H.2
  • 2
    • 77954917015 scopus 로고    scopus 로고
    • Celastrol acts as a potent antimetastatic agent targeting β1 integrin and inhibiting cell-extracellular matrix adhesion, in part via the p38 mitogen-activated protein kinase pathway
    • Zhu, H.; Liu, X. W.; Cai, T. Y.; Cao, J.; Tu, C. X.; Lu, W.; He, Q. J.; Yang, B. Celastrol acts as a potent antimetastatic agent targeting β1 integrin and inhibiting cell-extracellular matrix adhesion, in part via the p38 mitogen-activated protein kinase pathway. J. Pharmacol. Exp. Ther. 2010, 334, 489-499.
    • (2010) J. Pharmacol. Exp. Ther. , vol.334 , pp. 489-499
    • Zhu, H.1    Liu, X.W.2    Cai, T.Y.3    Cao, J.4    Tu, C.X.5    Lu, W.6    He, Q.J.7    Yang, B.8
  • 3
    • 0036065039 scopus 로고    scopus 로고
    • Benefit of an extract of Tripterygium wilfordii Hook F in patients with rheumatoid arthritis: A double-blind, placebocontrolled study
    • Tao, X.; Younger, J.; Fan, F. Z.; Wang, B.; Lipsky, P. E. Benefit of an extract of Tripterygium wilfordii Hook F in patients with rheumatoid arthritis: A double-blind, placebocontrolled study. Arthritis Rheum. 2002, 46, 735-743.
    • (2002) Arthritis Rheum. , vol.46 , pp. 735-743
    • Tao, X.1    Younger, J.2    Fan, F.Z.3    Wang, B.4    Lipsky, P.E.5
  • 5
    • 23844529468 scopus 로고    scopus 로고
    • Celastrol protects against MPTP- and 3-nitropropionic acid-induced neurotoxicity
    • DOI 10.1111/j.1471-4159.2005.03253.x
    • Cleren, C.; Calingasan, N. Y.; Chen, J.; Beal, M. F. Celastrol protects against MPTP-and 3-nitropropionic acidinduced neurotoxicity. J. Neurochem. 2005, 94, 995-1004. (Pubitemid 41170587)
    • (2005) Journal of Neurochemistry , vol.94 , Issue.4 , pp. 995-1004
    • Cleren, C.1    Calingasan, N.Y.2    Chen, J.3    Beal, M.F.4
  • 7
    • 42649088411 scopus 로고    scopus 로고
    • Celastrol inhibits the growth of human glioma xenografts in nude mice through suppressing VEGFR expression
    • Huang, Y. L.; Zhou, Y. X.; Fan, K. S.; Zhou, D. Celastrol inhibits the growth of human glioma xenografts in nude mice through suppressing VEGFR expression. Cancer Lett. 2008, 264, 101-106.
    • (2008) Cancer Lett. , vol.264 , pp. 101-106
    • Huang, Y.L.1    Zhou, Y.X.2    Fan, K.S.3    Zhou, D.4
  • 8
    • 78650733125 scopus 로고    scopus 로고
    • Natural proteasome inhibitor celastrol suppresses androgen-independent prostate cancer progression by modulating apoptotic proteins and NF-kappaB
    • Dai, Y.; DeSano, J.; Tang, W. H.; Meng, X. J.; Meng, Y.; Burstein, E.; Lawrence, T. S.; Xu, L. A. Natural proteasome inhibitor celastrol suppresses androgen-independent prostate cancer progression by modulating apoptotic proteins and NF-kappaB. PLoS One 2010, 5, e14153.
    • (2010) PLoS One , vol.5
    • Dai, Y.1    DeSano, J.2    Tang, W.H.3    Meng, X.J.4    Meng, Y.5    Burstein, E.6    Lawrence, T.S.7    Xu, L.A.8
  • 9
    • 0346220388 scopus 로고    scopus 로고
    • Bioactivation of herbal constituents: Simple alerts in the complex system
    • Zhou, S.; Koh, H. L.; Gao, Y.; Gong, Z. Y.; Lee, E. J. Bioactivation of herbal constituents: Simple alerts in the complex system. Life Sci. 2004, 74, 935-968.
    • (2004) Life Sci. , vol.74 , pp. 935-968
    • Zhou, S.1    Koh, H.L.2    Gao, Y.3    Gong, Z.Y.4    Lee, E.J.5
  • 10
    • 0031472588 scopus 로고    scopus 로고
    • Role of pharmacokinetics and metabolism in drug discovery and development
    • Lin, J. H.; Lu, A. Y. H. Role of pharmacokinetics and metabolism in drug discovery and development. Pharmacol. Rev. 1997, 49, 403-449. (Pubitemid 28030947)
    • (1997) Pharmacological Reviews , vol.49 , Issue.4 , pp. 403-449
    • Lin, J.H.1    Lu, A.Y.H.2
  • 11
    • 49949113587 scopus 로고    scopus 로고
    • Structure-activity relationship and substrate-dependent phenomena in effects of ginsenosides on activities of drug-metabolizing P450 enzymes
    • Hao, M.; Zhao, Y.; Chen, P.; Huang, H.; Liu, H.; Jiang, H.; Zhang, R.; Wang, H. Structure-activity relationship and substrate-dependent phenomena in effects of ginsenosides on activities of drug-metabolizing P450 enzymes. PLoS One 2008, 3, e2697.
    • (2008) PLoS One , vol.3
    • Hao, M.1    Zhao, Y.2    Chen, P.3    Huang, H.4    Liu, H.5    Jiang, H.6    Zhang, R.7    Wang, H.8
  • 12
    • 79551670426 scopus 로고    scopus 로고
    • Identification of cytochrome P450 (CYP) isoforms involved in metabolism of corynoline and assessment of its herb-drug interaction
    • Fang, Z. Z.; Zhang, Y. Y.; Ge, G. B.; Liang, S. C.; Sun, D. X.; Zhu, L. L.; Dong, P. P.; Cao, Y. F.; Yang, L. Identification of cytochrome P450 (CYP) isoforms involved in metabolism of corynoline and assessment of its herb-drug interaction. Phytother. Res. 2011, 25, 256-263.
    • (2011) Phytother. Res. , vol.25 , pp. 256-263
    • Fang, Z.Z.1    Zhang, Y.Y.2    Ge, G.B.3    Liang, S.C.4    Sun, D.X.5    Zhu, L.L.6    Dong, P.P.7    Cao, Y.F.8    Yang, L.9
  • 13
    • 77955646498 scopus 로고    scopus 로고
    • Inhibitory effects of curcumenol on human liver cytochrome P450 enzymes
    • Sun, D. X.; Fang, Z. Z.; Zhang, Y. Y.; Cao, Y. F.; Yang, L.; Yin, J. Inhibitory effects of curcumenol on human liver cytochrome P450 enzymes. Phytother. Res. 2010, 24, 1213-1216.
    • (2010) Phytother. Res. , vol.24 , pp. 1213-1216
    • Sun, D.X.1    Fang, Z.Z.2    Zhang, Y.Y.3    Cao, Y.F.4    Yang, L.5    Yin, J.6
  • 14
    • 84855215453 scopus 로고    scopus 로고
    • Inhibition of cytochrome P450 2C8-mediated drug metabolism by the flavonoid diosmetin
    • Quintieri, L.; Palatini, P.; Moro, S.; Floreani, M. Inhibition of cytochrome P450 2C8-mediated drug metabolism by the flavonoid diosmetin. Drug Metab. Pharmacokinet. 2011, 26, 559-568.
    • (2011) Drug Metab. Pharmacokinet. , vol.26 , pp. 559-568
    • Quintieri, L.1    Palatini, P.2    Moro, S.3    Floreani, M.4
  • 16
    • 15244342411 scopus 로고    scopus 로고
    • UDP-glucuronosyltransferases and clinical drug-drug interactions
    • DOI 10.1016/j.pharmthera.2004.10.013
    • Kiang, T. K.; Ensom, M. H.; Chang, T. K. UDP-glucuronosyltransferases and clinical drug-drug interactions. Pharmacol. Ther. 2005, 106, 97-132. (Pubitemid 40386722)
    • (2005) Pharmacology and Therapeutics , vol.106 , Issue.1 , pp. 97-132
    • Kiang, T.K.L.1    Ensom, M.H.H.2    Chang, T.K.H.3
  • 17
    • 0034534895 scopus 로고    scopus 로고
    • Roles of glucuronidation and UDP-glucuronosyltransferases in xenobiotic bioactivation reactions
    • DOI 10.1016/S0009-2797(00)00198-8, PII S0009279700001988
    • Ritter, J. K. Roles of glucuronidation and UDP-glucuronosyltransferasesin xenobiotic bioactivation reactions. Chem. Biol. Interact. 2000, 129, 171-193. (Pubitemid 32061059)
    • (2000) Chemico-Biological Interactions , vol.129 , Issue.1-2 , pp. 171-193
    • Ritter, J.K.1
  • 18
    • 0034128936 scopus 로고    scopus 로고
    • Human UDP-glucuronosyltransferases: Metabolism, expression, and disease
    • DOI 10.1146/annurev.pharmtox.40.1.581
    • Tukey, R. H.; Strassburg, C. P. Human UDP-glucuronosyltransferases: metabolism, expression, and disease. Annu. Rev. Pharmacol. Toxicol. 2000, 40, 581-616. (Pubitemid 30340694)
    • (2000) Annual Review of Pharmacology and Toxicology , vol.40 , pp. 581-616
    • Tukey, R.H.1    Strassburg, C.P.2
  • 19
    • 84855684309 scopus 로고    scopus 로고
    • Investigation of UDP-glucuronosyltransferases (UGT) inhibitory properties of carvacrol
    • Dong, R. H.; Fang, Z. Z.; Zhu, L. L.; Liang, S. C.; Ge, G. B.; Yang, L.; Liu, Z. Y. Investigation of UDP-glucuronosyltransferases (UGT) inhibitory properties of carvacrol. Phytother. Res. 2012, 26, 86-90.
    • (2012) Phytother. Res. , vol.26 , pp. 86-90
    • Dong, R.H.1    Fang, Z.Z.2    Zhu, L.L.3    Liang, S.C.4    Ge, G.B.5    Yang, L.6    Liu, Z.Y.7
  • 20
    • 84862975973 scopus 로고    scopus 로고
    • Evidence that unsaturated fatty acids are potent inhibitors of renal UDP-glucuronosyltransferases (UGT): Kinetic studies using human kidney cortical microsomes and recombinant UGT1A9 and UGT2B7
    • Tsoutsikos, P.; Miners, J. O.; Stapleton, A.; Thomas, A.; Sallustio, B. C.; Knights, K. M. Evidence that unsaturated fatty acids are potent inhibitors of renal UDP-glucuronosyltransferases (UGT): kinetic studies using human kidney cortical microsomes and recombinant UGT1A9 and UGT2B7. Biochem. Pharmacol. 2010, 65, 919-921.
    • (2010) Biochem. Pharmacol. , vol.65 , pp. 919-921
    • Tsoutsikos, P.1    Miners, J.O.2    Stapleton, A.3    Thomas, A.4    Sallustio, B.C.5    Knights, K.M.6
  • 21
    • 34848893895 scopus 로고    scopus 로고
    • Inhibitory effects of adenine nucleotides and related substances on UDP-glucuronosyltransferase: Structure-effect relationships and evidence for an allosteric mechanism
    • DOI 10.1016/j.bbagen.2007.07.011, PII S0304416507001614
    • Nishimura, Y.; Maeda, S.; Ikushiro, S.; Mackenzie, P. I.; Ishii, Y.; Yamada, H. Inhibitory effects of adenine nucleotides and related substances on UDP-glucuronosyltransferase: structure-effect relationships and evidence for an allosteric mechanism. Biochim. Biophys. Acta 2007, 1770, 1557-1566. (Pubitemid 47503557)
    • (2007) Biochimica et Biophysica Acta - General Subjects , vol.1770 , Issue.11 , pp. 1557-1566
    • Nishimura, Y.1    Maeda, S.2    Ikushiro, S.-i.3    Mackenzie, P.I.4    Ishii, Y.5    Yamada, H.6
  • 22
    • 0023112104 scopus 로고
    • Paracetamol as a test drug to determine glucuronide formation in man. Effects of inducers and of smoking
    • DOI 10.1007/BF00541295
    • Bock, K. W.; Wiltfang, J.; Blume, R.; Ullrich, D.; Bircher, J. Paracetamol as a test drug to determine glucuronide formation in man. Effects of inducers and of smoking. Eur. J. Clin. Pharmacol. 1987, 31, 677-683. (Pubitemid 17020998)
    • (1987) European Journal of Clinical Pharmacology , vol.31 , Issue.6 , pp. 677-683
    • Bock, K.W.1    Wiltfang, J.2    Blume, R.3
  • 23
    • 0037324354 scopus 로고    scopus 로고
    • Serotonin (5-hydroxytryptamine) glucuronidation in vitro: Assay development, human liver microsome activities and species differences
    • DOI 10.1080/0049825021000048809
    • Krishnaswamy, S.; Duan, S. X.; von Moltke, L. L.; Greenblatt, D. J.; Sudmeier, J. L.; Bachovchin, W. W.; Court, M. H. Serotonin (5-hydroxytryptamine) glucuronidation in vitro: Assay development, human liver microsome activities and species differences. Xenobiotica 2003, 33, 169-180. (Pubitemid 36237939)
    • (2003) Xenobiotica , vol.33 , Issue.2 , pp. 169-180
    • Krishnaswamy, S.1    Duan, S.X.2    Von Moltke, L.L.3    Greenblatt, D.J.4    Sudmeier, J.L.5    Bachovchin, W.W.6    Court, M.H.7
  • 24
    • 0038685671 scopus 로고    scopus 로고
    • Validation of serotonin (5-hydroxtryptamine) as an in vitro substrate probe for human UDP-glucuronosyltransferase (UGT) 1A6
    • DOI 10.1124/dmd.31.1.133
    • Krishnaswamy, S.; Duan, S. X.; von Moltke, L. L.; Court, M. H. Validation of serotonin (5-hydroxtryptamine) as an in vitro substrate probe for human UDP-glucuronosyltransferase (UGT) 1A6. Drug. Metab. Dispos. 2003, 31, 133-139. (Pubitemid 36735267)
    • (2003) Drug Metabolism and Disposition , vol.31 , Issue.1 , pp. 133-139
    • Krishnaswamy, S.1    Duan, S.X.2    Von Moltke, L.L.3    Greenblatt, D.J.4    Court, M.H.5
  • 25
    • 1842536833 scopus 로고    scopus 로고
    • Human UDP-glucuronosyltransferases: Isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid
    • DOI 10.1124/dmd.32.4.413
    • Uchaipichat, V.; Mackenzie, P. I.; Guo, X. H.; Gardner-Stephen, D.; Galetin, A.; Houston, J. B.; Miners, J. O. Human UDP-glucuronosyltransferases: Isoform selectivity and kinetics of 4-methylumbelliferone and 1-naphthol glucuronidation, effects of organic solvents, and inhibition by diclofenac and probenecid. Drug. Metab. Dispos. 2004, 32, 413-423. (Pubitemid 38420275)
    • (2004) Drug Metabolism and Disposition , vol.32 , Issue.4 , pp. 413-423
    • Uchaipichat, V.1    Mackenzie, P.I.2    Guo, X.-H.3    Gardner-Stephen, D.4    Galetin, A.5    Houston, J.B.6    Miners, J.O.7
  • 26
    • 84863002608 scopus 로고    scopus 로고
    • Correlation analysis of secondary metabolites and environmental factors in Tripterygium wilfordii
    • Du, W.; Huang, H. Correlation analysis of secondary metabolites and environmental factors in Tripterygium wilfordii. Acta Bot. Sin. 2008, 25, 707-713.
    • (2008) Acta Bot. Sin. , vol.25 , pp. 707-713
    • Du, W.1    Huang, H.2


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